The most commonly reported side effects of tocilizumab include rheumatoid arthritis, off label use, and pain, based on 115,903 FDA adverse event reports from 2005 to 2025. 30.3% of reports found the drug to be ineffective.
Percentages show how often each reaction appears relative to total reports for tocilizumab.
These are voluntary reports and do not establish that tocilizumab caused these reactions.
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Other drugs that appear in adverse event reports alongside tocilizumab. Drugs flagged as a suspected cause appear in the first column. Drugs taken at the same time but not suspected appear in the second.
Also suspected
Taken alongside
Co-occurrence in adverse event reports does not establish a drug interaction. Patients often take multiple medications, and these lists reflect prescribing patterns rather than causal relationships. Consult a healthcare provider about potential drug interactions.
68.4% of tocilizumab adverse event reports involve female patients and 19.6% involve male patients. The largest age group is adult at 61%. These figures reflect who reports side effects, not underlying risk.
Sex
Age group
Conditions and purposes for which patients were taking tocilizumab when the adverse event was reported.
Showing 15 of 1,409 indications
Tocilizumab is sold under brand names including Actemra, Tofidence, Tyenne.
An upward trend reflects increased FAERS reporting overall, not necessarily increased risk.
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